HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthalenethiol → HCID 178418688, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthalenethiol | HCID 7058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178418938 | HCID 178418938 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178418688 | HCID 178418688 | — |
Reaction Steps
To a solution of (5-cyclopropyl-2H-pyrazol-3-yl)-(2,6-dichloropyrimidin-4-yl)-amine (211 mg, 0.781 mmol) and 2-naphthalenethiol (125-mg, 0.781 mmol) in tert-butanol (5 mL) was added triethylamine (174 μL, 1.25 mmol) and the resulting mixture was heated at reflux for 15 hours. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, Hexane/AcOEt gradient) to afford (6-chloro-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-cyclopropyl-2H-pyrazol-3-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531536B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f023398d2d48451a99ba07f213c1f376 |
| Source note | uspto-grants-2009_05 |